|Publication number||US5055373 A|
|Application number||US 07/414,342|
|Publication date||Oct 8, 1991|
|Filing date||Sep 29, 1989|
|Priority date||Sep 29, 1988|
|Publication number||07414342, 414342, US 5055373 A, US 5055373A, US-A-5055373, US5055373 A, US5055373A|
|Inventors||Keiso Saeki, Fumiaki Shinozaki, Toshiaki Endo|
|Original Assignee||Fuji Photo Film Co., Ltd.|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (13), Referenced by (80), Classifications (25), Legal Events (6)|
|External Links: USPTO, USPTO Assignment, Espacenet|
This invention relates to a non-silver salt type multicolor recording material and, more particularly, to a light- and/or heat-sensitive multicolor recording material using leuco dyes capable of being colored by oxidation.
As the most popular process for obtaining multicolor images, silver salt photography has been widely put into practice from the viewpoint of high sensitivity, high image quality, excellent gradation reproducibility, etc. However, the silver salt photography has the defect that it requires complicated steps since it involves the steps of imagewise exposure, processing with a developer, and conversion of remaining silver halide to a water-soluble silver complex salt or to a silver salt stable to light.
In order to remove the above problems, JP-A-59-48764 (The term "JP-A" as used herein means an "unexamined published Japanese patent application"), etc. describe dry-process silver salt photographic light-sensitive materials; British Patent 249,530 and U.S. Pat. Nos. 2,020,775, 2,004,625, 2,217,544, 2,255,463 and 2,699,394, etc. describe dye diffusion transfer process photographic light-sensitive materials; and U.S. Pat. No. 2,844,574, etc. describe silver dye bleach process photographic light-sensitive materials.
On the other hand, as recording materials not using silver salts, there have been employed an electrophotographic system in which an apparatus is equipped with multicolor recording mechanism, a thermal transfer system, an ink-jet system, and the like. However, these systems have such deficiencies as that large-sized equipment is required, that recording reliability is insufficient, and that exchange of expendables is troublesome.
Since a thermal recording system does not involve the above-described problems, multicolor recording materials of that type of system would be quite easy to use. As a conventional process employing the thermal recording system, there has been a process wherein a plurality of color-forming units successively undergo color formation reaction as heat energy applied thereto is increased to give hues based on color mixing as described in JP-B-51-19989 (corresponding to U.S. Pat. No. 3,895,173) (the term "JP-B" as used herein means an "examined Japanese patent publication"), JP-B-52-11231, JP-A-54-88135, JP-A-55-133991, JP-A-55-133992, etc. As another process, there has been a process wherein a decolorizing mechanism of allowing a decolorising agent to act on a color-forming unit capable of forming color at a lower temperature simultaneously when a color-forming unit having a higher heat response temperature forms color is employed as described in, for example, JP-B-50-17868 (corresponding to U.S. Pat. No. 3,843,384), JP-B-51-5791, JP-B-57-14318 and JP-B-57-14319. However, these techniques have the defect that the number of hues capable of being formed is small, which is a fatal defect for a color hard copy.
As multicolor recording materials overcoming the above-described defects, recording materials wherein heat-sensitive coloration system, light-sensitive coloration system, etc. are combined are described in Japanese Patent Application Nos. 61-80787 (corresponding to U.S. Patent Ser. No. 07/174306), JP-A-63-172681, JP-A-63-45084 (corresponding to U.S. Patent Ser. No. 07/174306), JP-A-63-134282 (corresponding to U.S. Patent Ser. No. 07/125675), etc. These comprise a transparent support having provided on one side thereof at least one color-forming unit layer and on the other side at least one color-forming unit layer capable of forming a color of different hue from that of the above-described unit layer, said color-forming units containing a combination of a diazo compound and a coupler as a color-forming component and/or a combination of a leuco dye and a colordeveloper as a color-forming component. However, these recording materials unavoidably employ a transparent support for providing color-forming unit layers on both sides thereof because formation of a plurality of color-forming unit layers on the same side causes problems with respect to their shelf life, image density, etc. Therefore, there is a limitation that an opaque support cannot be used, and a disadvantage in producing them that an opaque layer must be additionally provided. In addition, upon formation of an image, thermal printing must be conducted from both sides of the recording material, and hence they have the defect of requiring a complicated recording apparatus.
It is, therefore, an object of the present invention to provide a multicolor recording material which comprises a support having provided on one and the same side thereof a color-forming layer, and which has an excellent shelf life and provides an excellent coloration density.
The above described object of the present invention can be attained by a multicolor recording material, which comprises a support having provided thereon a coating layer comprising two or more kinds of microcapsules each containing at least a leuco dye capable of being colored by oxidation and a photo oxidizing agent, and a reducing agent outside of the microcapsules as necessary components, with two or more leuco dyes capable of forming different colors from each other being retained in different kinds of said microcapsules respectively composed of walls of high polymers having different glass transition points.
A process of using the multicolor recording material of the present invention to obtain a good multicolor image is described below.
Let the glass transition points of the walls of mixed microcapsules be T1, T2, . . . , Tn from the lower side, wavelengths for causing coloration by the leuco dyes and the photo oxidants be λ1, λ2, . . . , λn and colored hues be C1, C2, . . . , Cn, respectively.
If λ1, λ2, . . . , λn are different from each other, an image with a hue of C1 can be obtained by thermally printing at a temperature of T1 ≦T<T2 using, for example, a thermal block (printing temperature; T) to form a latent image, then exposing it with a light of λ1. Subsequently, thermal printing is conducted at T2 ≦T<T3 to form a latent image, then exposure is conducted using a light of λ2 in wavelength to form an image with a hue of C2. After repeating this procedure with the final thermal printing being conducted at T≦Tn followed by exposure with a light of λn, there can be obtained an image with a hue of Cn.
In the above-described case, the order of the thermal printing and the exposure may be reversed. That is, an image may be formed by exposure, followed by fixing by heat to obtain a similar multicolor image.
If λ1, λ2, . . . , λn are the same, a good multicolor image can be obtained by successively conducting thermal printing with changing the heating temperature using, for example, a thermal block to form a latent image, then exposing all over the recording material. In this case, individual hues cannot be independently obtained, and a mixed-color image is formed.
In the present invention, preferable capsules prevent a substance existing inside the capsule and a substance outside the capsule from coming into contact with each other by the separating function of the microcapsule wall at an ordinary (room and/or storage) temperature and, only when heated to a temperature higher than a certain level, show an increased permeability for such substances. This phenomenon permits one to freely control the permeation-initiating temperature by properly selecting capsule wall-forming materials, capsule core materials, and additives. In this situation, the permeation-initiating temperature corresponds to the glass transition temperature of the capsule wall.
The term "glass transition temperature" used herein means a temperature at which a viscoelasticity of a high polymer is rapidly changed as described, for example, in Kagaku Dai-Jiten (Chemical Encyclopedia), published by Kyowa Shuppan K. K., .vol. 2, pp. 523-524 (1987).
In view of sufficient thermal recording, the glass transition temperature is preferably 60° to 200° C. and, in order to obtain rapid response to instant heat by a thermal head, it is more preferably 70° to 150° C.
In order to control the glass transition temperature intrinsic to the capsule wall, it is necessary to change the kind of capsule wall-forming material. As the wall-forming material to be used in the present invention, there are illustrated polyurethane, polyurea, polyamide, polyester, polycarbonate, etc., with polyurethane and polyurea being particularly preferred.
Microcapsules to be used in the present invention are formed by emulsifying a core substance containing image-forming substances such as a leuco dye and a photo oxidant, and forming a high polymer substance wall around the emulsified oil droplets. In this case, wall-forming reactants are added to the inside and/or outside of the oil droplets.
As a process for forming microcapsule walls of the present invention, a microencapsulation process by polymerization of reactants from inside of the oil droplets enables one to obtain, particularly within a short time, microcapsules of uniform size capable of forming recording materials with an excellent shelf life.
Techniques of microencapsulation, materials and specific examples of compounds to be used are described in U.S. Pat. Nos. 3,726,804 and 3,796,696.
For example, in the case of using polyurethane or polyurea as a capsule wall-forming material, a polyisocyanate and a second substance capable of reacting with the polyisocyanate to form capsule wall (for example, polyol or polyamine) are mixed in an aqueous phase or in an oily liquid to be encapsulated, and the resulting solution is emulsified and dispersed in water, followed by increasing the temperature to cause a high polymer-forming reaction at the interface of oily droplets for forming the microcapsule wall.
Glass transition point of the capsule wall can be greatly changed by properly selecting the first wall-forming substance, polyisocyanate, and the second wall-forming substance, polyol or polyamine.
As an organic solvent for dissolving the above-described image-forming substances, high-boiling oils are used. Specific examples thereof include phosphoric acid esters, carboxylic acid esters such as phthalic acid esters, acrylic acid esters and methacrylic acid esters, fatty acid amides, alkylated biphenyls, alkylated terphenyls, alkylated naphthalenes, diarylethanes, chlorinated paraffins, etc.
In the present invention, the above-described organic solvents may be used in combination with a low-boiling auxiliary solvent. Specific examples of the auxiliary solvent include ethyl acetate, isopropyl acetate, butyl acetate, methylene chloride, cyclohexanone, etc.
In order to form stable emulsified oil droplets, a protective colloid or a surfactant may be added to the aqueous phase. As the protective colloid, water-soluble high polymers are generally usable.
In the present invention, microcapsules have preferably a size of up to 20μ, more preferably up to 4μ, in volume average value in view of improvement of resolving power of image and handling ease.
The leuco dye constituting one component of the image-forming material of the present invention is of a reduced form of a dye having one or two hydrogen atoms which, when the hydrogen atom or atoms are removed therefrom or in some cases an additional electron or electrons are added thereto, forms a color, thus forming a dye. Such leuco dye is substantially colorless or is slightly colored, and hence it gives a means for forming a pattern when oxidized to form color. In the present invention, this oxidation is attained by allowing at least one photo oxidant to coexist with the leuco dye. This photo oxidant is activated by irradiation with light, then reacts with the leuco dye to form a colored image against the non-irradiated background and therefore unchanges areas.
The leuco dye which can be easily colored by the above-described mechanism includes, for example, those which are described in U.S. Pat. No. 3,445,234 and are illustrated below:
(10) Aminohydrocinnamic acid (cyanoethane, leucomethine);
(12) Leucoindigoid dyes;
(15) 2-(p-Hydroxyphenyl)-4,5-diphenylimidazole; and
Of these leuco dyes, (1) to (9) form dyes when they lose one hydrogen atom, and (10) to (16) form dyes when they lose two hydrogen atoms.
Specifically, there can be illustrated Leuco Crystal Violet, tris-(4-diethylamino-o-tolyl)-methane, bis-(4-diethylamino-o-tolyl)-phenylmethane, bis-(4-diethylamino-o-tolyl)-thienyl-2-methane, bis-(2-chloro-4-diethylaminophenyl)-phenylmethane, 2-(2-chlorophenyl)amino-6-N,N-dibutylamino-9-(2-methoxycarbonyl)-phenylxanthene, 2-N,N-dibenzylamino-6-N,N-diethylamino-9-(2-methoxycarbonyl)-phenylxanthene, benzo(a)-6-N,N-diethylamino-9-(2-methoxycarbonyl)-phenylxanthene, 2 -(2-chlorophenyl)-amino-6-N,N-dibutylamino-9-(2-methylphenylcarboxamido)-phenylxanthene, 3,6-dimethoxy-9-(2-methoxycarbonyl)-phenylxanthene, 3,6-diethoxyethyl-9-(2-methoxycarbonyl)-phenylxanthene, benzoyl leucomethylene blue, 3,7-bis-diethylaminophenoxazine, etc.
On the other hand, preferable photo oxidants to be used as the image-forming materials of the present invention are those which are usually inactive but, when irradiated with actinic radiation such as visible light rays, ultraviolet rays, infrared rays or X rays, produce a chemical substance capable of oxidizing the leuco dyes to their colored forms.
As typical examples of the photo oxidants, there are illustrated lophine dimer compounds such as 2,4,5-triarylimidazole dimers described in JF D-62-39728 (corresponding to U.S. Pat. No. 4,247,618) and JP-B-63-2099 (corresponding to U.S. Pat. Nos. 4,311,783 and 4,252,887); azide compounds such as 2-azidobenzoxazole, benzoylazide and 2-azidobenzimidazole described in U.S. Pat. No. 3,282,693; pyridinium compound such as 3'-ethyl-1-methoxy-2-pyridothiacyanine perchlorate and 1-methoxy-2-methylpyridinium p-toluenesulfonate, and organic halogen compounds such as N-bromosuccinimide, tribromo methyl phenyl sulfone, 2-trichloromethyl-5-(p-butoxystyryl)-1,3,4-oxadiazole and 2,6-ditrichloromethyl-4-(p-methoxyphenyl)triazine, described in U.S. Pat. No. 3,615,568; azide polymers described in Photographic Society of Japan, Collection of Abstracts of Lectures for Study Presentation Held in Spring, page 55 (1968). Of these compounds, lophine dimer compounds and organic halogen compounds are preferable, with a combination of the two being particularly preferable since it provides a high sensitivity.
In preparing the image-forming material of the present invention, the leuco dye and the photo oxidant are mixed in a proportion of preferably 10:1 to 1:10, more preferably 2:1 to 1:2, in molar ratio.
The image-forming material of the present invention forms a stable latent image when subjected to heating treatment, and provides a stable image when subsequently subjected to all-over exposure, or when subjected to exposure to form an image and then to the heating treatment. That is, the thermal recording or fixing mechanism of the image-forming material of the present invention is that, upon being heated, the photo oxidant comes into contact with a reducing agent through the capsule wall and, therefore, even when the photo oxidant is activated thereafter, the activated photo oxidant will soon be deactivated by the action of the reducing agent.
Such reducing agent functions as a so-called free radical scavenger which traps the free radical of the activated photo oxidant.
As specific examples of the reducing agent, there are illustrated hydroquinone compounds and aminophenol compounds which have a hydroxy group in the benzene ring and at least another hydroxy group or amino group in a different position of the benzene ring, described in U.S. Pat. No. 3,042,515, cyclic phenylhydrazide compounds described in JP-B-62-39728, and compounds selected from among guanidine derivatives, alkylenediamine derivatives and hydroxyamine derivatives. These compounds may be used alone or as a combination of two or more. However, these are not limitative at all, and those reducing substances which possess the function of acting on the oxidants may also be used.
In the image-forming material of the present invention, the above-described reducing agents are used in a state of being solid-dispersed by sand mill or the like or in a state of being dissolved in an oil and emulsified and dispersed. Upon solid dispersion or emulsion dispersion of the reducing agent, a water-soluble high polymer can generally be employed as a protective colloid.
The reducing agent is used in an amount of preferably 1 to 100 mols, more preferably 5 to 20 mols, per mol of the photo oxidant component.
In the present invention, known sensitizing agents, ultraviolet ray absorbents and anti-oxidants may be used as additional components for the photo oxidant.
In addition, aids may be used for the purpose of freely controlling the thermal recording or thermal fixing. Such aids function to decrease the melting point of individual components constituting the system or decrease glass transition points of the capsule walls.
Such aids include phenol compounds, alcohol compounds, amide compounds, sulfonamide compounds, etc. These compounds may be incorporated in the core substance or may be added as a dispersion outside the microcapsules.
The image-forming material in accordance with the present invention can be prepared by coating on a support a dispersion of microcapsules retaining a leuco dye and a photo oxidant, and with a reducing agent outside the microcapsules.
In this occasion, a binder, a pigment, a wax, a metallic powder or a surfactant may be added to the above-described dispersion.
As to the coating amount of the image-forming layer in the present invention, an amount of 3 to 30 g/m2, particularly 5 to 20 g/m2, is preferable.
As materials suited as a support, there are illustrated papers of from tissue paper to thick board, regenerated cellulose, cellulose acetate, cellulose nitrate, polyethylene terrephthalate, polyethylene, polyvinyl acetate, polymethyl methacrylate and polyvinyl chloride.
As coating methods for coating the dispersion on the support, there are illustrated an air-knife coating method, a curtain coating method, a slide coating method, a roller coating method, a dip-coating method, a wire-bar coating method, a blade coating method, a gravure coating method, a spin coating method and an extrusion coating method which, however, are not limitative at all.
In the present invention, formation of a latent image by heating is absolutely the same as with ordinary heat-sensitive recording as described, for example, in U.S. Pat. Nos. 4,436,920 and 4,480,052 and may be conducted by using a thermal pen or a thermal head.
In the present invention, all of convenient light sources may be employed for activation of the photo oxidant and formation of leuco dye image. Conventional light sources include a fluorescent lamp, a mercury lamp, a metal halide lamp, a xenon lamp, a tungsten lamp, etc.
The multicolor recording material of the present invention is characterized in that it is excellent in shelf life and coloration density and that, since only one recording layer is required, steps for producing it can be markedly simplified.
The present invention is now illustrated in more detail by reference to the following examples which, however, are not to be construed as limiting the present invention in any way.
Additionally, "parts" showing an amount to be added are by weight.
EXAMPLE 1______________________________________Preparation of Capsule Solution A______________________________________Leuco Crystal Violet 1 part2,2'-Bis-(o-chlorophenyl)-4,4',5,5'- 2 partstetraphenylimidazoleTribromomethyl phenyl sulfone 0.4 part2,5-Di-tert-octylhydroquinone 0.6 partp-Toluenesulfonamide 0.2 part75 wt % solution of xylylenediisocyanate/ 20 partstrimethylolpropane adduct in ethylacetate______________________________________
The above-described ingredients were added to a mixed solvent of 16 parts of ethyl acetate and 18 parts of diisopropylnaphthalene to dissolve them. The resulting solution was added to 54 parts of a 6 wt % aqueous solution of carboxy-modified polyvinyl alcohol, and emulsified and dispersed at 20° C. to obtain an emulsion of 1μ in average particle size. 68 parts of water was added to the resulting emulsion, and the mixture was stirred at 40° C. for 3 hours. Subsequently, the temperature of the mixture was restored to room temperature, followed by filtration of it to obtain a capsule solution A.
The glass transition point of this capsule wall was 80° C., and a wavelength for coloration by the leuco dye and the photo oxidant was 365 nm, with the coloration hue being blue.
______________________________________Preparation of Capsule Solution B______________________________________3,6-Dimethoxy-9-(2-methoxy- 1.5 partscarbonyl)-phenylxanthene2,2-Bis-(o-chlorophenyl)-4,4',5,5'- 2 partstetraphenylimidazole2,6-Ditrichloromethyl-4- 0.8 part(p-methoxyphenyl)-triazine2-(5'-Methyl-2'-hydroxyphenyl)- 4 partsbenzotriazole75 wt % solution of tolylenediiso- 20 partscyanate/trimethylolpropane adductin ethyl acetate______________________________________
The above-described ingredients were added to a mixed solvent of 16 parts of ethyl acetate and 18 parts of diisopropylnaphthalene to dissolve them. The resulting solution was added to 54 parts of a 6 wt % aqueous solution of carboxy-modified polyvinyl alcohol, and emulsified and dispersed at 20° C. to obtain an emulsion of 1μ in average particle size. 68 parts of water was added to the resulting emulsion, and the mixture was stirred at 40° C. for 3 hours. Subsequently, the temperature of the mixture was restored to room temperature, followed by filtration of it to obtain a capsule solution B.
The glass transition point of this capsule wall was 100° C., and a wavelength for coloration by the leuco dye and the photo oxidant was 435 nm, with the coloration hue being yellow.
30 parts of 1-phenylpyrazolidin-3-one (Phenidone A) was added to 150 parts of a 4 wt % aqueous solution of carboxy-modified polyvinyl alcohol, then subjected to dispersing step using a horizontal sand mill to obtain a Phenidone A dispersion having an average particle size of 1μ m.
Then, a coating solution of the following formulation was prepared.
______________________________________Capsule solution A described above 6.8 partsCapsule solution B described above 6.8 partsReducing agent dispersion described 6.0 partsabove30% epoxydated polyamide resin 0.4 part(FL-71, product of Toho ChemicalIndustry Co., Ltd.)______________________________________
This coating solution was coated on woodfree paper (basis weight: 76 g/m2) in a solid amount of 12 g/m2, then dried at 50° C. to obtain a multicolor recording material of the present invention.
Several portions of the thus obtained recording sheet was heated at random at 80° C. for one second using a thermal block, then the sheet was irradiated all over for 5 seconds using a jet light (ultra high-pressure mercury lamp, made by ORC) through a filter intercepting light of 400 nm or more to obtain a blue-color image.
Further, the recording material was heated at 100° C. for one second using a thermal block, then irradiated all over for 5 seconds using a jet light through a filter intercepting light of 400 nm or less to obtain a yellow-color image formed in the image-forming layer.
As a result, there was obtained a distinct color image having the color of blue, yellow and black (blue+yellow).
While the present invention has been described in detail and with reference to specific embodiments thereof, it is apparent to one skilled in the art that various changes and modifications can be made therein without departing from the spirit and scope of the present invention.
|Cited Patent||Filing date||Publication date||Applicant||Title|
|US4529681 *||Nov 17, 1983||Jul 16, 1985||Fuji Photo Film Co., Ltd.||Light- and heat-sensitive recording material|
|US4772541 *||Oct 10, 1986||Sep 20, 1988||The Mead Corporation||Photohardenable compositions containing a dye borate complex and photosensitive materials employing the same|
|US4800149 *||Feb 16, 1988||Jan 24, 1989||The Mead Corporation||Photohardenable compositions containing a dye borate complex and photosensitive materials employing the same|
|US4816368 *||Feb 9, 1987||Mar 28, 1989||The Mead Corporation||Microencapsulated photosensitive compositions employing image forming initiators|
|US4874684 *||Sep 3, 1987||Oct 17, 1989||Fuji Photo Film Co., Ltd.||Light-sensitive material containing silver halide, reducing agent and polymerizable compound in microcapsules separately sensitized|
|US4924009 *||Jun 3, 1987||May 8, 1990||Bowling Green State University||Xanthene dye complexes|
|US4929530 *||Mar 16, 1989||May 29, 1990||Fuji Photo Film Co., Ltd.||Light image forming material and image-recording method using such|
|US4935329 *||Jun 1, 1988||Jun 19, 1990||The Mead Corporation||Negative working imaging process employing photosensitive microcapsules|
|US4942107 *||Mar 8, 1989||Jul 17, 1990||Fuji Photo Film Co., Ltd.||Image-forming material and image recording method using the same|
|DE3908692A1 *||Mar 16, 1989||Oct 5, 1989||Fuji Photo Film Co Ltd||Aufzeichnungsmaterial und aufzeichnungsverfahren unter verwendung desselben|
|GB2113860A *||Title not available|
|GB2198253A *||Title not available|
|JPS57124343A *||Title not available|
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US5582957||Mar 28, 1995||Dec 10, 1996||Eastman Kodak Company||Resuspension optimization for photographic nanosuspensions|
|US6387584 *||Dec 11, 1996||May 14, 2002||Fuji Photo Film Co., Ltd.||Photoimaging material|
|US6759366||Dec 18, 2001||Jul 6, 2004||Ncr Corporation||Dual-sided imaging element|
|US6784906||Dec 18, 2001||Aug 31, 2004||Ncr Corporation||Direct thermal printer|
|US6801233||May 20, 2002||Oct 5, 2004||Polaroid Corporation||Thermal imaging system|
|US6906735||Oct 4, 2004||Jun 14, 2005||Polaroid Corporation||Thermal imaging system|
|US7166558||Mar 23, 2004||Jan 23, 2007||Zink Imaging, Llc||Thermal imaging system|
|US7531224||Jul 20, 2007||May 12, 2009||Ncr Corporation||Two-sided thermal transfer ribbon|
|US7589752||Dec 21, 2005||Sep 15, 2009||Ncr Corporation||Two-sided thermal printing|
|US7635660||Apr 3, 2006||Dec 22, 2009||Zink Imaging, Inc.||Thermal imaging system|
|US7710442||Feb 23, 2007||May 4, 2010||Ncr Corporation||Two-sided thermal print configurations|
|US7764299||Feb 2, 2007||Jul 27, 2010||Ncr Corporation||Direct thermal and inkjet dual-sided printing|
|US7777770||Mar 6, 2007||Aug 17, 2010||Ncr Corporation||Dual-sided two-ply direct thermal image element|
|US7791626||Jan 30, 2008||Sep 7, 2010||Zink Imaging, Inc.||Print head pulsing techniques for multicolor printers|
|US7808674||May 28, 2008||Oct 5, 2010||Zink Imaging, Inc.||Image stitching for a multi-head printer|
|US7830405||Jun 23, 2005||Nov 9, 2010||Zink Imaging, Inc.||Print head pulsing techniques for multicolor printers|
|US7839425||Sep 17, 2008||Nov 23, 2010||Ncr Corporation||Method of controlling thermal printing|
|US8043993||Nov 14, 2006||Oct 25, 2011||Ncr Corporation||Two-sided thermal wrap around label|
|US8067335||Nov 9, 2006||Nov 29, 2011||Ncr Corporation||Multisided thermal media combinations|
|US8072644||Sep 1, 2010||Dec 6, 2011||Zink Imaging, Inc.||Image stitching for a multi-head printer|
|US8083423||Mar 1, 2006||Dec 27, 2011||Ncr Corporation||Thermal indicators|
|US8098269||Sep 1, 2010||Jan 17, 2012||Zink Imaging, Inc.||Print head pulsing techniques for multicolor printers|
|US8114812||Mar 3, 2006||Feb 14, 2012||Ncr Corporation||Two-sided thermal paper|
|US8164609||Nov 5, 2010||Apr 24, 2012||Zink Imaging, Inc.||Print head pulsing techniques for multicolor printers|
|US8173575||Feb 8, 2007||May 8, 2012||Ncr Corporation||Dual-sided thermal form card|
|US8182161||Aug 31, 2007||May 22, 2012||Ncr Corporation||Controlled fold document delivery|
|US8194107||Jun 4, 2007||Jun 5, 2012||Ncr Corporation||Two-sided thermal print command|
|US8211826||Aug 6, 2007||Jul 3, 2012||Ncr Corporation||Two-sided thermal media|
|US8222184||Oct 16, 2006||Jul 17, 2012||Ncr Corporation||UV and thermal guard|
|US8252717||Dec 17, 2008||Aug 28, 2012||Ncr Corporation||Dual-sided two-ply direct thermal image element|
|US8314821||Nov 22, 2010||Nov 20, 2012||Ncr Corporation||Method of controlling thermal printing|
|US8345307||Dec 6, 2011||Jan 1, 2013||Zink Imaging, Inc.||Image stitching for a multi-head printer|
|US8377844||Aug 3, 2009||Feb 19, 2013||Zink Imaging, Inc.||Thermally-insulating layers and direct thermal imaging members containing same|
|US8462184||Jun 4, 2007||Jun 11, 2013||Ncr Corporation||Two-sided thermal printer control|
|US8502846||Mar 19, 2012||Aug 6, 2013||Zink Imaging, Inc.||Print head pulsing techniques for multicolor printers|
|US8504427||Sep 28, 2007||Aug 6, 2013||Ncr Corporation||Multi-lingual two-sided printing|
|US8576436||Jun 20, 2007||Nov 5, 2013||Ncr Corporation||Two-sided print data splitting|
|US8670009||Dec 22, 2006||Mar 11, 2014||Ncr Corporation||Two-sided thermal print sensing|
|US8721202||Feb 16, 2007||May 13, 2014||Ncr Corporation||Two-sided thermal print switch|
|US8848010||Aug 7, 2007||Sep 30, 2014||Ncr Corporation||Selective direct thermal and thermal transfer printing|
|US9024986||Aug 11, 2006||May 5, 2015||Ncr Corporation||Dual-sided thermal pharmacy script printing|
|US9056488||Jul 18, 2007||Jun 16, 2015||Ncr Corporation||Two-side thermal printer|
|US20040180284 *||Mar 23, 2004||Sep 16, 2004||Polaroid Corporation||Thermal imaging system|
|US20050052521 *||Oct 4, 2004||Mar 10, 2005||Polaroid Corporation||Thermal imaging system|
|US20060270552 *||Apr 3, 2006||Nov 30, 2006||Zink Imaging, Llc||Thermal imaging system|
|US20060289633 *||Jun 23, 2005||Dec 28, 2006||Ncr Corporation||Receipts having dual-sided thermal printing|
|US20060290769 *||Jun 23, 2005||Dec 28, 2006||Polaroid Corporation||Print head pulsing techniques for multicolor printers|
|US20070120942 *||Nov 30, 2005||May 31, 2007||Ncr Corporation||Dual-sided two color thermal printing|
|US20070120943 *||Nov 30, 2005||May 31, 2007||Ncr Corporation||Dual-sided thermal printing with labels|
|US20070134039 *||Dec 8, 2005||Jun 14, 2007||Ncr Corporation||Dual-sided thermal printing|
|US20070206982 *||Mar 1, 2006||Sep 6, 2007||Ncr Corporation||Thermal indicators|
|US20070207926 *||Mar 3, 2006||Sep 6, 2007||Ncr Corporation||Two-sided thermal paper|
|US20070210572 *||Oct 13, 2006||Sep 13, 2007||Ncr Corporation||Dual-sided thermal security features|
|US20070211094 *||Aug 11, 2006||Sep 13, 2007||Ncr Corporation||Dual-sided thermal pharmacy script printing|
|US20070211099 *||Dec 22, 2006||Sep 13, 2007||Lyons Dale R||Two-sided thermal print sensing|
|US20070211132 *||Feb 23, 2007||Sep 13, 2007||Lyons Dale R||Two-sided thermal print configurations|
|US20070211134 *||Feb 2, 2007||Sep 13, 2007||Ncr Corporation||Direct thermal and inkjet dual-sided printing|
|US20070211135 *||Mar 6, 2007||Sep 13, 2007||Richard Moreland||Dual-sided two-ply direct thermal image element|
|US20070212146 *||Feb 16, 2007||Sep 13, 2007||Dale Lyons||Two-sided thermal print switch|
|US20070212515 *||Feb 8, 2007||Sep 13, 2007||Ncr Corporation||Dual-sided thermal form card|
|US20070213213 *||Oct 16, 2006||Sep 13, 2007||Ncr Corporation||UV and thermal guard|
|US20070213214 *||Nov 14, 2006||Sep 13, 2007||Roth Joseph D||Two-sided thermal wrap around label|
|US20070213215 *||Dec 4, 2006||Sep 13, 2007||Ncr Corporation||Multi-color dual-sided thermal printing|
|US20070244005 *||Nov 9, 2006||Oct 18, 2007||Ncr Corporation||Multisided thermal media combinations|
|US20080225308 *||May 28, 2008||Sep 18, 2008||Zink Imaging, Llc||Image stitching for a multi-head printer|
|US20080238967 *||Jan 30, 2008||Oct 2, 2008||Zink Imaging, Llc||Print head pulsing techniques for multicolor printers|
|US20080297583 *||Jun 4, 2007||Dec 4, 2008||Dale Lyons||Two-sided thermal print command|
|US20090015647 *||Jul 18, 2007||Jan 15, 2009||Rawlings Timothy W||Two-side thermal printer|
|US20090017237 *||Jul 20, 2007||Jan 15, 2009||Rawlings Timothy W||Two-sided thermal transfer ribbon|
|US20090058892 *||Aug 31, 2007||Mar 5, 2009||Ncr Corporation||Direct thermal and inkjet dual-sided printing|
|US20090060606 *||Aug 31, 2007||Mar 5, 2009||Ncr Corporation||Controlled fold document delivery|
|US20090089172 *||Sep 28, 2007||Apr 2, 2009||Quinlan Mark D||Multi-lingual two-sided printing|
|US20090185021 *||Feb 23, 2007||Jul 23, 2009||Lyons Dale R||Two-sided thermal print configurations|
|US20090290923 *||Nov 26, 2009||Dale Lyons||Two-sided thermal print switch|
|US20100087316 *||Aug 3, 2009||Apr 8, 2010||Day John C||Thermally-Insulating Layers and Direct Thermal Imaging Members Containing Same|
|US20100253716 *||Jun 17, 2010||Oct 7, 2010||Ncr Corporation||Direct thermal and inkjet dual-sided printing|
|US20110050830 *||Nov 5, 2010||Mar 3, 2011||Zink Imaging, Inc.||Print head pulsing techniques for multicolor printers|
|US20110063394 *||Nov 22, 2010||Mar 17, 2011||Morrison Randall L||Method of controlling thermal printing|
|US20110085185 *||Sep 1, 2010||Apr 14, 2011||Zink Imaging, Llc||Image stitching for a multi-head printer|
|WO1998019868A1 *||Nov 5, 1997||May 14, 1998||Olav Marcus Aagaard||Process for the manufacture of an object with a coloured marking|
|U.S. Classification||430/138, 430/203, 503/204, 428/402.21, 430/541, 503/214, 430/916, 430/913, 428/402.2|
|International Classification||G03C1/675, G03C1/73, B41M5/30, G03C5/56, G03C1/00, G03F7/004, B41M5/28, G03F7/00|
|Cooperative Classification||Y10T428/2985, Y10T428/2984, Y10S430/114, Y10S430/117, G03C1/002, G03F7/002|
|European Classification||G03F7/00M, G03C1/00M|
|Sep 29, 1989||AS||Assignment|
Owner name: FUJI PHOTO FILM CO., LTD., 210, NAKANUMA, MINAMI A
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNORS:SAEKI, KEISO;SHINOZAKI, FUMIAKI;ENDO, TOSHIAKI;REEL/FRAME:005147/0551
Effective date: 19890918
|Apr 4, 1995||FPAY||Fee payment|
Year of fee payment: 4
|Mar 29, 1999||FPAY||Fee payment|
Year of fee payment: 8
|Oct 10, 1999||LAPS||Lapse for failure to pay maintenance fees|
|Dec 21, 1999||FP||Expired due to failure to pay maintenance fee|
Effective date: 19991008
|Mar 17, 2003||FPAY||Fee payment|
Year of fee payment: 12